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Ethyl 2,2-dimethylbutanoate, also known as ethyl 2,2-dimethylpropionate, is an organic compound with the chemical formula C7H14O2. It is a colorless liquid with a fruity, apple-like odor and is commonly used as a flavoring agent in the food and beverage industry. This ester is formed by the reaction of ethanol and 2,2-dimethylbutanoic acid, and it is characterized by its molecular structure, which includes a central carbon atom bonded to two methyl groups, an ethyl group, and a carboxylate group. Ethyl 2,2-dimethylbutanoate is soluble in most organic solvents and has a relatively low boiling point, making it suitable for use in various industrial applications.

5129-40-8

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5129-40-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5129-40-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,2 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5129-40:
(6*5)+(5*1)+(4*2)+(3*9)+(2*4)+(1*0)=78
78 % 10 = 8
So 5129-40-8 is a valid CAS Registry Number.

5129-40-8Relevant academic research and scientific papers

TETRAHYDROTRIAZOLOPYRIDINE COMPOUNDS AS SELECTIVE MGLU5 RECEPTOR POTENTIATORS USEFUL FOR THE TREATMENT OF SCHIZOPHRENIA

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Page/Page column 21, (2011/07/30)

The present invention provides certain tetrahydrotriazolopyridine derivatives, pharmaceutical compositions thereof, methods of using the same and processes for preparing the same. Formula (I) wherein R1 is hydrogen, fluoro, chloro, or methyl; and R2 is C4 - CS branched alkyl.

Deconjugative Alkylation of α,β-Acetylenic Esters by Electrogenerated Base

Tokuda, Masao,Nishio, Osamu

, p. 1592 - 1596 (2007/10/02)

Electrolysis of ethyl propiolate (1) and an excess of methyl iodide at a platinum cathode in hexamethylphosphoric triamide (HMPA) or N,N-dimethylformamide (DMF) solution containing tetra-n-butylammonium salt gave the acetylenic esters 2, 3, and 4.Similar electrochemical reactions of α,β-acetylenic esters 2, 5, and 9 with methyl iodide took place in good yields to give the corresponding α,α-dimethyl-β,γ-acetylenic esters 3 and 4, 4, and 10, respectively.Electrochemical reactions of 5 with ethyl, butyl, and allyl iodides also gave α,α-dialkyl β,γ-acetylenic esters 6, 7, and 8, respectively.These facile deconjugative alkylations appeared to take place by the action of the electrogenerated base (EGB) which was formed by the electrochemical reduction of alkyl iodides.Alkyl iodides worked as both a probasic compound of the EGB and as an electrophile.Reaction pathways of the present deconjugative alkylations are also discussed.

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